In this varied and highly responsible position, your technical expertise is required to ensure the optimal performance of our advanced pharmaceutical machinery and equipment at customer sites worldwide. A key focus of this role is the professional execution and documentation of GMP‑compliant qualification and calibration activities.
Your role in our team
Independent execution of installation, commissioning, maintenance, inspection and repair work on our pharmaceutical equipment
Troubleshooting and analysis of electrical, electronic and mechatronic components
Implementation of technical adjustments and modifications according to internal specifications
Execution, evaluation and documentation of qualifications and calibrations on our pharmaceutical systems
Calibration of key measurement parameters
Verification of measurement results according to defined tolerances and documentation of deviations (OOT/OOS)
Initiation and implementation of corrective and preventive actions
GMP‑compliant preparation of calibration protocols, service reports and technical documentation
Support during qualification procedures (e.g. IQ/OQ)
Technical support during customer and regulatory audits
Instruction and training of customer personnel
Close collaboration with our Technical Service Support team and internal departments
Support for production and other technical service areas as needed
Your profile
You are a strong communicator, customer‑oriented and confident in your technical expertise. Thanks to your structured, analytical and solution‑oriented approach, you are comfortable working independently.
Completed training in electronics, electrical engineering, mechatronics or a related field
Experience in pharmaceutical engineering or other regulated industries (pharma, biotech, medical devices) is an advantage
Knowledge of calibration processes and measurement technology is desirable
Basic understanding of GMP, GAMP5 and documentation‑intensive work environments
Confident in handling measurement and test equipment
High level of accuracy, quality awareness and technical understanding
Strong analytical thinking and manual dexterity
Excellent communication and customer orientation
Flexibility, adaptability and resilience
Strong commitment and ability to concentrate
Very good English skills
Willingness to travel (>70%) and to accept short‑notice assignments. Please note: Permission to travel within EU / USA is a prerequisite for this role
Your working environment
You will support leading pharmaceutical manufacturers worldwide. Our systems operate in highly regulated cleanroom environments, where precision, reliability and compliance are essential. In this position, you will gain deep insights into pharmaceutical technologies, GMP standards and complex system architectures while contributing to safe and high‑quality pharmaceutical production.
Your Benefits
You will work in an exciting and international environment with customers and colleagues from around the world
We offer you individual long‑term development opportunities in exciting and technically challenging projects
A new dedicated company vehicle that can be used 7 days a week
You will gain expertise in state‑of‑the‑art industry technologies
Our modern office is conveniently located at the Dublin GEC - Ireland’s largest global entrepreneurial superhub
You will have access to a pension scheme
You will have access to a comprehensive health insurance plan
We offer flexible working time models including home office
Apply now and join our team!
Ready for your next step? Click on ‘Apply now’ to get started right away! As long as the position is advertised, you can apply at any time. We value diversity and therefore welcome all applicants – regardless of gender, nationality, ethnic or social origin, religion/belief, disability, age, sexual orientation and identity, and any other protected status. You can find out more about our culture here Culture at Körber – it's worth taking a look! If you have any questions or technical problems, please send us an e‑mail to jobs@koerber.com. Larissa Franz is the responsible person for this job advertisement. We work with permanent partners and therefore ask recruitment consultants to refrain from contacting us by e‑mail or telephone.
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